CLC-6, a member of the CLC family of voltage-gated chloride channels and transporters, plays a pivotal role in the physiological regulation of cellular chloride homeostasis. The gene encoding CLC-6 is expressed in various tissues, with notable prevalence in neuronal and renal systems. The protein's function is essential for maintaining the electrochemical gradient of chloride ions across cell membranes, a process vital to numerous cellular operations, including volume regulation, signal transduction, and acidification of intracellular organelles. Regulation of CLC-6 expression, therefore, is a subject of considerable interest in the study of cellular ion balance. The transcriptional control of CLC-6 is complex and can be influenced by a multitude of factors at the genetic level. Epigenetic modifications such as DNA methylation and histone acetylation, along with transcription factor binding, are among the fundamental mechanisms that can potentially induce the expression of this protein. Understanding the factors that can elevate the transcription of CLC-6 may provide insights into the cellular processes that govern chloride channel expression and function.
Several biochemical compounds have been identified that could influence the expression of CLC-6 through various intracellular signaling pathways and epigenetic mechanisms. For instance, retinoic acid is known to interact with nuclear receptors that can enhance gene transcription, potentially increasing the expression of proteins like CLC-6. Similarly, forskolin, by raising intracellular cAMP, may activate protein kinases that phosphorylate transcription factors, leading to the transcriptional activation of the CLC-6 gene. Epigenetic modifiers, such as 5-Azacytidine and Trichostatin A, can cause DNA demethylation and histone acetylation respectively, potentially leading to the upregulation of CLC-6. Moreover, signaling molecules like Epidermal Growth Factor (EGF) and activators of protein kinase C, such as Phorbol 12-myristate 13-acetate (PMA), can initiate a cascade of cellular events culminating in enhanced gene expression. While the detailed molecular interactions of these compounds with the CLC-6 gene remain an active area of research, they are thought to promote the transcription of CLC-6 through their respective pathways. It is through the intricate interplay of such biomolecules and cellular signaling events that the expression of crucial proteins like CLC-6 is finely tuned within the cellular environment.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
Retinoic acid may stimulate the transcriptional events that elevate the expression of genes including CLC-6 by engaging with retinoic acid receptors. | ||||||
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $76.00 $150.00 $725.00 $1385.00 $2050.00 | 73 | |
Forskolin's elevation of intracellular cAMP levels can activate CREB, which may lead to the transcriptional activation and subsequent upregulation of CLC-6 expression. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine inhibits DNA methyltransferases, potentially causing demethylation and reactivation of genes, which could include the gene encoding CLC-6, leading to its increased expression. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
Trichostatin A induces hyperacetylation of histones, which may enhance transcriptional activity of genes including that of CLC-6 by making the chromatin more accessible. | ||||||
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $40.00 $129.00 $210.00 $490.00 $929.00 | 119 | |
PMA activates PKC, which might trigger a signaling cascade that promotes the transcriptional activation of genes, potentially stimulating an increase in CLC-6 expression. | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $30.00 $46.00 $82.00 $218.00 | 19 | |
Sodium butyrate's inhibition of histone deacetylases may result in an open chromatin structure, promoting gene transcription and potentially leading to the upregulation of CLC-6 expression. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $76.00 $82.00 $367.00 | 36 | |
Dexamethasone binds to glucocorticoid receptors, which may act as transcription factors to enhance the expression of target genes, including the gene encoding CLC-6. | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Lithium chloride's disruption of inositol monophosphatase activity could lead to stimulation of pathways that upregulate gene expression, potentially including the gene for CLC-6. | ||||||
Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $36.00 $68.00 $107.00 $214.00 $234.00 $862.00 $1968.00 | 47 | |
Curcumin's activation of transcription factors like NF-κB can promote the transcription of a variety of genes, potentially initiating an increase in CLC-6 expression. | ||||||
2-Deoxy-D-glucose | 154-17-6 | sc-202010 sc-202010A | 1 g 5 g | $65.00 $210.00 | 26 | |
As an inhibitor of glucose metabolism, 2-Deoxy-D-glucose can activate stress response pathways such as AMPK, which may lead to the transcriptional upregulation of genes including those related to CLC-6. |